That's like saying that Iron is made of electrons.
Sure, neurons have electrons in them, but they are mostly protons and neutrons by mass. When VitalOne tries to make an entire cell subject to the quantum effects of single electrons he makes a leap not supported by any know process. In other words, he is making stuff up.
Besides, the workings of the cell are mostly chemical, not quantum. Once atoms bond with each other based on valence properties, the molecules react according to shape and shape alone. There is a very deterministic (some might even say Newtonian) way in which molecules interact based on shape and the sharing of electrons in outer orbits. So predictable that my computer crunches these shapes and interactions in its spare time. And since my computer is not a quantum computer...
...look, both of you guys aren't just wrong about all of this. You are speaking insanity.
Respectfully yours.
Did not read the article I linked, did you?
Try again:
Trans-plasma membrane electron transport is critical for maintaining cellular redox balance and viability, yet few, if any, investigations have studied it in intact primary neurons. In this investigation, extracellular reduction of 2,6-dichloroindophenol (DCIP) and ferricyanide (FeCN) were measured as indicators of trans-plasma membrane electron transport by chick forebrain neurons. Neurons readily reduced DCIP, but not FeCN unless CoQ1, an exogenous ubiquinone analog, was added to the assays. CoQ1 stimulated FeCN reduction in a dose-dependent manner but had no effect on DCIP reduction. Reduction of both substrates was totally inhibited by ε-maleimidocaproic acid (MCA), a membrane-impermeant thiol reagent, and slightly inhibited by superoxide dismutase. Diphenylene iodonium, a flavoenzyme inhibitor, completely inhibited FeCN reduction but had no affect on DCIP reduction, suggesting that these substrates are reduced by distinct redox pathways. The relationship between plasma membrane electron transport and neuronal viability was tested using the inhibitors MCA and capsaicin. MCA caused a dose-dependent decline in neuronal viability that closely paralleled its inhibition of both reductase activities. Similarly capsaicin, a NADH oxidase inhibitor, induced a rapid decline in neuronal viability. These results suggest that trans-plasma membrane electron transport helps maintain a stable redox environment required for neuronal viability.
And additionally:
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=534007the membranes of the biological organism are liquid crystalline in character. The liquid crystalline state of matter is particularly temperature sensitive. This sensitivity defines the biologically viable temperature range. Within its operating range, the liquid crystalline state of matter exhibits unique properties. The crystalline characteristics associated with that state contribute to the quantum physical characteristics of these membranes.
http://64.233.161.104/search?q=cach...ane&hl=en&gl=us&ct=clnk&cd=8&client=firefox-a
Shape and shape alone?
http://www.ncbi.nlm.nih.gov/entrez/..._uids=16603141&query_hl=3&itool=pubmed_DocSum
Lipid headgroup conformations in protein crystals also do not conform solely to the bent-down conformation, with gauche-gauche configuration of the phospho-diester, that is characteristic of phospholipid bilayer membranes. This suggests that the lipids that are resolved in crystals of membrane proteins are not representative of the entire lipid-protein interface. Much of the chain configurational disorder of the membrane-bound lipids in crystals arises from energetically disallowed skew conformations. This indicates a configurational heterogeneity in the lipids at a single binding site: eclipsed conformations occur also in some glycerol backbone torsion angles and C-C torsion angles in the lipid headgroups. Stereochemical violations in the protein-bound lipids are evidenced by one-third of the ester carboxyl groups in non-planar configurations, and certain of the carboxyls in the cis configuration. Some of the lipid structures in protein crystals have the incorrect enantiomeric configuration of the glycerol backbone, and many of the branched methyl groups in structures of the phytanyl chains associated with bacteriorhodopsin crystals are in the incorrect S-configuration.
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